| Product NDC: | 15338-170 |
| Proprietary Name: | Folic Acid |
| Non Proprietary Name: | Folic Acid |
| Active Ingredient(s): | 1 mg/1 & nbsp; Folic Acid |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 15338-170 |
| Labeler Name: | Apace Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA080680 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20091223 |
| Package NDC: | 15338-170-00 |
| Package Description: | 48 BOTTLE in 1 CARTON (15338-170-00) > 100 TABLET in 1 BOTTLE |
| NDC Code | 15338-170-00 |
| Proprietary Name | Folic Acid |
| Package Description | 48 BOTTLE in 1 CARTON (15338-170-00) > 100 TABLET in 1 BOTTLE |
| Product NDC | 15338-170 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Folic Acid |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20091223 |
| Marketing Category Name | NDA |
| Labeler Name | Apace Packaging |
| Substance Name | FOLIC ACID |
| Strength Number | 1 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |